| Disease #03937 (IHPRF1 (hypotonia, infantile, with psychomotor retardation and characteristic facies, type 1 (IHPRF-1)), OMIM:615419)
        
          | Official abbreviation | IHPRF1 |  
          | Name | hypotonia, infantile, with psychomotor retardation and characteristic facies, type 1 (IHPRF-1) |  
          | OMIM ID | 615419 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal recessive |  
          | Individuals reported having this disease | 5 |  
          | Phenotype entries for this disease | 4 |  
          | Associated with 1 gene | NALCN |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2014-09-25 23:29:40 +02:00 (CEST) |  
          | Date last edited | 2021-12-10 21:51:32 +01:00 (CET) |  
 
 Individuals
 |